Separating photosynthetic pigments by chromatography

Molecules (Interaction and interdependence) · Photosynthesis · note 2 of 9

Separating photosynthetic pigments by chromatographySpec C1.3.4

In short

Chromatography separates photosynthetic pigments because each pigment has a different solubility in the solvent and attraction to the paper or thin-layer plate, so they travel different distances. Pigments are identified by colour and by Rf value, which is the distance moved by the pigment divided by the distance moved by the solvent front. Paper or thin-layer chromatography can be used.

Leaves contain several photosynthetic pigments. They can be separated by chromatography, using paper or a thin-layer chromatography (TLC) plate. Each pigment travels a different distance because it differs in how soluble it is in the solvent and how strongly it is attracted to the stationary phase.

  1. Grind leaf tissue with a little sand and propanone (or another suitable solvent) to extract the pigments.
  2. Draw a pencil origin line about 1 cm from the bottom of the paper or plate.
  3. Apply a small, concentrated spot of extract to the origin, letting it dry between applications.
  4. Stand the paper or plate in a small depth of running solvent, below the origin, in a covered container.
  5. Remove it when the solvent is near the top and immediately mark the solvent front with pencil.
  6. Mark the centre of each pigment spot, measure distances from the origin and calculate Rf values.
Rf = distance moved by pigment ÷ distance moved by solvent front

Rf values are always between 0 and 1 and have no units. Pigments are identified by their colour and by comparing their Rf values with reference values for the same solvent and stationary phase.

Common photosynthetic pigments and their colours
PigmentColour on the chromatogram
CaroteneOrange-yellow (usually travels furthest)
XanthophyllsYellow
Chlorophyll aBlue-green
Chlorophyll bYellow-green

Calculating an Rf value

On a chromatogram the solvent front moved 8.0 cm from the origin. A blue-green spot moved 4.4 cm. Calculate its Rf value.

  1. Rf = distance moved by pigment ÷ distance moved by solvent front.
  2. Rf = 4.4 ÷ 8.0 = 0.55.

Answer: Rf = 0.55 (no units). With its blue-green colour this is likely chlorophyll a; confirm with reference values for the same method.

Practical skill:

Use a pencil for the origin (ink would separate too), keep the origin above the solvent, and measure to the centre of each spot. Rf values depend on the solvent and medium, so only compare with references from the same method.

Finished chromatogram strip with a pencil origin line and a solvent front; four pigment spots from top: carotene (orange-yellow), xanthophyll (yellow), chlorophyll a (blue-green) and chlorophyll b (yellow-green); arrows mark the distance moved by a pigment and by the solvent, with Rf = distance moved by pigment ÷ distance moved by solvent. (opens full size in a new tab)
A typical chromatogram of leaf pigments (illustrative positions; order and Rf values depend on the solvent and medium). ==Rf = pigment distance ÷ solvent distance==.

Written and checked against the IB Biology HL specification · Updated October 2026

Frequently asked questions

Why do plants absorb red and blue light but not green?

Chlorophyll absorbs mainly red and blue light because only photons with energy matching the gaps between its electron energy levels can excite its electrons. Green light does not match well, so most of it is reflected or transmitted, which is why leaves look green. Accessory pigments such as carotenoids absorb some other wavelengths.

What is the difference between an absorption spectrum and an action spectrum?

An absorption spectrum shows the percentage of light a pigment absorbs at each wavelength, while an action spectrum shows the rate of photosynthesis at each wavelength. Both peak in blue and red light. The action spectrum stays above zero in green light because accessory pigments absorb some of it, and the similar shapes show absorbed light drives photosynthesis.

How do you calculate Rf values in chromatography?

Divide the distance moved by the pigment by the distance moved by the solvent front, both measured from the origin line. Rf values lie between 0 and 1 and have no units. Pigments are identified by their colour and by comparing their Rf values with reference values for the same solvent and medium.

All 5 questions on Photosynthesis